Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7302444 | Neuroscience & Biobehavioral Reviews | 2018 | 25 Pages |
Abstract
In this review on SIB phenomenology in people with ID in general and in twelve genetic syndromes, we summarize different SIB characteristics across these etiologically distinct entities and identify influencing factors. We demonstrate that the prevalence of SIB in several well-known genetic intellectual disability syndromes is noticeably higher than in individuals with ID in general, and that characteristics such as age of onset and topographies differ widely across syndromes. Each syndrome is caused by a mutation in a different gene, and this allows detection of several pathways that lead to SIB. Studying these with the behavioral consequences as specific aim will be an important step toward targeted early interventions and prevention.
Keywords
Interdisciplinary studyPainSelf-injurious behaviorGenesAngelman SyndromeLesch-Nyhan syndromePrader-Willi syndromefragile X syndromeSmith-Magenis syndromeDown syndromeLowe syndromeGenetic syndromesWilliams-Beuren syndromeCornelia de Lange SyndromeRett syndromeCri du Chat Syndromeintellectual disability
Related Topics
Life Sciences
Neuroscience
Behavioral Neuroscience
Authors
Sylvia Huisman, Paul Mulder, Janneke Kuijk, Myrthe Kerstholt, Agnies van Eeghen, Arnold Leenders, Ingrid van Balkom, Chris Oliver, Sigrid Piening, Raoul Hennekam,